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Evidence for classification of c.1852_1853AA > GC in MLH1 as a neutral variant for Lynch syndrome 

Castillejo, Adela; Guarinos, Carla; Martínez Canto, Ana; Barberá, Víctor Manuel; Egoavil, Cecilia; Castillejo, María Isabel; Pérez Carbonell, Lucía; Sánchez Heras, Ana Beatriz; Segura, Angel; Ochoa, Enrique; Lázaro, Rafael; Ruiz Ponte, Clara; Bujanda Fernández de Pierola, Luis; Andreu, Montserrat; Castells, Antoni; Carracedo, Angel; Llor, Xavier; Clofent, Juan; Alenda, Cristina; Paya, Artemio; Jover, Rodrigo; Soto, José Luis (BioMed Central, 2011-01)
Background: Lynch syndrome (LS) is an autosomal dominant inherited cancer syndrome characterized by early onset cancers of the colorectum, endometrium and other tumours. A significant proportion of DNA variants in LS ...

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AuthorAlenda, Cristina (1)Andreu, Montserrat (1)Barberá, Víctor Manuel (1)
Bujanda Fernández de Pierola, Luis (1)
... View MoreDepartamento (cas.)
Medicina (1)
Departamento (eus.)Medikuntza (1)SubjectGENETICS AND HEREDITY (1)... View MoreDate Issued
2011 (1)
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eng (1)

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